Canonical Allele Identifier: CA1751305403
Gene:

Linked Data

dbSNP Id: rs181226542

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148561011C>A , CM000669.2:g.148561011C>A GRCh38
NC_000007.13:g.148258103C>A , CM000669.1:g.148258103C>A GRCh37
NC_000007.12:g.147889036C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928099.1:n.300+7089G>T
XR_928100.1:n.433+7089G>T